Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's Feet Lines

PHASE3CompletedINTERVENTIONAL
Enrollment

446

Participants

Timeline

Start Date

October 1, 2010

Primary Completion Date

April 1, 2011

Study Completion Date

July 1, 2011

Conditions
Lateral Canthus RhytidesCrow's Feet Lines
Interventions
BIOLOGICAL

onabotulinumtoxinA

24 units onabotulinumtoxinA (botulinum toxin Type A) total dose injected into bilateral Crow's Feet Line areas on Day 1

DRUG

normal saline

Injected into bilateral Crow's Feet Line areas on Day 1

Trial Locations (4)

Unknown

Newport Beach

Aalst

Vancouver

Sutton Coldfield

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Allergan

INDUSTRY